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Volumn 135, Issue 33, 2013, Pages 12188-12191

Cyclopentannulation of Conjugated Enones Using a Vinyldiazomethane-Based Reagent

Author keywords

[No Author keywords available]

Indexed keywords

1 ,3-DIPOLE; BIFUNCTIONAL REAGENTS; CONJUGATED ENONES; CYCLOPENTANNULATION; DIASTEREOSELECTIVE; DIKETONES; TWO STEP METHOD;

EID: 84883118176     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja4054866     Document Type: Article
Times cited : (15)

References (77)
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    • However, Doyle has described an annulation process based on the products of his annulation after conversion of the enol silane to the parent ketone: Zhang, Y.; Doyle, M. P. ARKIVOC 2010, viii, 10
    • (2010) ARKIVOC , vol.8 , pp. 10
    • Zhang, Y.1    Doyle, M.P.2
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    • 0032572862 scopus 로고    scopus 로고
    • (enol silyl ether cyclopropanation using Cu(I)-box complexes)
    • Ebinger, A.; Heinz, T.; Umbricht, G.; Pfaltz, A. Tetrahedron 1998, 54, 10469 (enol silyl ether cyclopropanation using Cu(I)-box complexes)
    • (1998) Tetrahedron , vol.54 , pp. 10469
    • Ebinger, A.1    Heinz, T.2    Umbricht, G.3    Pfaltz, A.4
  • 64
    • 33746696684 scopus 로고    scopus 로고
    • Oxycyclopropane fragmentation has been observed previously under the reaction conditions for cyclopropanation of enol ethers
    • Oxycyclopropane fragmentation has been observed previously under the reaction conditions for cyclopropanation of enol ethers: Muthusamy, S.; Srinivasan, P. Tetrahedron Lett. 2006, 47, 6297
    • (2006) Tetrahedron Lett. , vol.47 , pp. 6297
    • Muthusamy, S.1    Srinivasan, P.2
  • 65
    • 0028308010 scopus 로고
    • For a mechanistic study implicating electrophilic silicon as a catalyst in the Mukaiyama aldol reaction, see: Carreira, E. M; Singer, R. A. Tetrahedron Lett. 1994, 35, 4323
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4323
    • Carreira, E.M.1    Singer, R.A.2
  • 66
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    • Purification of β-siloxy-α,β-unsaturated enoates has been achieved by vacuum distillation, though is not general. Depressed isolated yields are observed upon attempted chromatographic purification. For example, see: Moody, C. J.; Taylor, R. J. J. Chem. Soc., Perkin Trans. 1 1989, 721
    • (1989) J. Chem. Soc., Perkin Trans. 1 , pp. 721
    • Moody, C.J.1    Taylor, R.J.2
  • 67
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    • For a timely discussion of the Buchner reaction in natural product total synthesis, see: Reisman, S. E.; Nani, R. R.; Levin, S. Synlett 2011, 2437
    • (2011) Synlett , pp. 2437
    • Reisman, S.E.1    Nani, R.R.2    Levin, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.